Evidence map›Paper›PMID 33290276›Full record

ArticleThe Journal of clinical investigation2021

Natural killer cells activated through NKG2D mediate lung ischemia-reperfusion injury.

Daniel R Calabrese, Emily Aminian, Benat Mallavia, Fengchun Liu, Simon J Cleary, Oscar A Aguilar, Ping Wang, Jonathan P Singer, Steven R Hays, Jeffrey A Golden and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 47 papers.

0numbers the graph read from it
0cells of the map it votes in
47citing papers in PubMed
2.4field-weighted citation impact, top 10% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

47 citing papers in PubMed, 64 citations in OpenAlex.

  1. Article
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  5. Activation of donor-derived eosinophils during static storage contributes to primary graft dysfunction after lung transplantation.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2026
    Article
  6. Article
  7. Immature neutrophils are elevated in human PGD and linked to G-CSF-driven injury in a murine model of lung ischemia-reperfusion.The Journal of heart and lung transplantation : the official publication of the International Society for Heart Transplantation · 2026
    Article
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  20. Airway epithelium in lung transplantation: a potential actor for post-transplant complications?European respiratory review : an official journal of the European Respiratory Society · 2024
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Daniel R CalabreseDepartment of Medicine, University of California, San Francisco, California.
Emily AminianDepartment of Medicine, University of California, San Francisco, California.
Benat MallaviaDepartment of Medicine, University of California, San Francisco, California.
Fengchun LiuDepartment of Medicine, University of California, San Francisco, California.
Simon J ClearyDepartment of Medicine, University of California, San Francisco, California.
Oscar A AguilarDepartment of Microbiology and Immunology, University of California, San Francisco, California.
Ping WangDepartment of Medicine, University of California, San Francisco, California.
Jonathan P SingerDepartment of Medicine, University of California, San Francisco, California.
Steven R HaysDepartment of Medicine, University of California, San Francisco, California.
Jeffrey A GoldenDepartment of Medicine, University of California, San Francisco, California.
Jasleen KukrejaDepartment of Surgery, University of California, San Francisco, California.
Daniel DuggerMedical Service, Veterans Affairs Health Care System, San Francisco, California.
Mary NakamuraDepartment of Medicine, University of California, San Francisco, California.
Lewis L LanierDepartment of Microbiology and Immunology, University of California, San Francisco, California.
Mark R LooneyDepartment of Medicine, University of California, San Francisco, California.
John R GreenlandDepartment of Medicine, University of California, San Francisco, California.
University of California, San Francisco · USSan Francisco VA Medical Center · US

Funding

Research BaseP30DK063720 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GERMAN, MICHAEL S · 2003 to 2019
$21.8M
NK MemoryR01AI068129 · NIAID · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LANIER, LEWIS LEE · 2006 to 2020
$6.0M
Platelet and megakaryocyte biology in the normal and injured lungR01HL107386 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2011 to 2020
$4.2M
Mechanisms of antibody-mediated lung Injury after blood transfusionR01HL138673 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS, ZIMRING, JAMES C. · 2019 to 2022
$2.3M
Innate Immune Mechanisms of Primary Graft Dysfunction after Lung TransplantationR01HL130324 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI LOONEY, MARK ROBERTS · 2016 to 2019
$2.2M
Telomere Dysfunction as a cause of Chronic Lung Allograft DysfunctionR01HL151552 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI GREENLAND, JOHN · 2020 to 2024
$1.6M
Cytek Aurora 5-Laser Spectral Flow CytometerS10OD026940 · OD · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI SIMOES MARTINS BISPO, CLAUDIA · 2019 to 2019
$341k
Cytomegalovirus Immune Responses in Chronic Lung Allograft Dysfunction PathogenesisI01CX002011 · VA · VETERANS AFFAIRS MED CTR SAN FRANCISCO · PI GREENLAND, JOHN · 2020 to 2025
–
BLRD VA IK2 BX005301CSRD VA I01 CX002011NHLBI NIH HHS K08 HL151761NHLBI NIH HHS R01 HL107386NHLBI NIH HHS R01 HL130324NHLBI NIH HHS R01 HL138673NHLBI NIH HHS R01 HL151552NIAID NIH HHS R01 AI068129NIDDK NIH HHS P30 DK063720NIH HHS S10 OD026940
6 · The paper itself

Abstract

Pulmonary ischemia-reperfusion injury (IRI) is a clinical syndrome of acute lung injury that occurs after lung transplantation or remote organ ischemia. IRI causes early mortality and has no effective therapies. While NK cells are innate lymphocytes capable of recognizing injured cells, their roles in acute lung injury are incompletely understood. Here, we demonstrated that NK cells were increased in frequency and cytotoxicity in 2 different IRI mouse models. We showed that NK cells trafficked to the lung tissue from peripheral reservoirs and were more mature within lung tissue. Acute lung ischemia-reperfusion injury was blunted in a NK cell-deficient mouse strain but restored with adoptive transfer of NK cells. Mechanistically, NK cell NKG2D receptor ligands were induced on lung endothelial and epithelial cells following IRI, and antibody-mediated NK cell depletion or NKG2D stress receptor blockade abrogated acute lung injury. In human lung tissue, NK cells were increased at sites of ischemia-reperfusion injury and activated NK cells were increased in prospectively collected human bronchoalveolar lavage in subjects with severe IRI. These data support a causal role for recipient peripheral NK cells in pulmonary IRI via NK cell NKG2D receptor ligation. Therapies targeting NK cells may hold promise in acute lung injury.

Indexed as

Lymphocyte ActivationAnimalsHumansKiller Cells, NaturalLungLung DiseasesMiceMice, KnockoutNK Cell Lectin-Like Receptor Subfamily KReperfusion InjuryKlrk1 protein, mouseNK Cell Lectin-Like Receptor Subfamily KImmunologyInnate immunityOrgan transplantationPulmonology

Identifiers

PMID33290276
PMCPMC7852842
OpenAlexW3111934078

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.